Verifying that our products meet all specifications and quality requirements
Quality Assurance (QA) is a way of preventing mistakes or defects in manufactured products, and avoiding problems when delivering solutions or services to customers. It’s important in order to verify that the products meet specifications and requirements.
Risk analysis at an early stage to validate the process
Quality, delivery precision and risk management are important for us as a solution provider in the medical device business. We always strive for the highest quality with great flexibility using validated production processes that ensure a high product quality.
Together with our customers we go through all possible risks at an early stage. We analyse, evaluate, control, and monitor the risks inherent in the medical technology products and components. We have established a medical device risk management process where we:
- Identify risks
- Estimate and evaluate these risks
- Develop and implement risk control measures
- Monitor the effectiveness of the risk management process
Extensive knowledge of the entire requirement set
Our strength lies within our extensive knowledge of the entire requirement set. We understand the market, the products, the medical device laws and regulations and the customer requirements as well as the requirements of the products. Our operators are well trained and accustomed to work with high quality standards. There are constantly ongoing dialogues about how we can optimize our quality processes and all decisions go through the quality department.